ClinVar Miner

Submissions for variant NM_033118.4(MYLK2):c.1082+19G>A

gnomAD frequency: 0.00002  dbSNP: rs745498112
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002101252 SCV002395979 likely benign Hypertrophic cardiomyopathy 1 2021-10-24 criteria provided, single submitter clinical testing

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